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FDA 510(k)

MEDAID

K-Number: K810841 · 1981-06-12

ApplicantC.V.I., Inc.
Decision Date1981-06-12
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDAID is the device name listed in this FDA 510(k) record. The listed applicant is C.V.I., Inc.. It received FDA 510(k) clearance on 1981-06-12 under 510(k) number K810841. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDAID?

MEDAID is a medical device that received FDA 510(k) clearance on 1981-06-12. The listed applicant is C.V.I., Inc.. The 510(k) number is K810841.

When did MEDAID receive FDA 510(k) clearance?

MEDAID received FDA 510(k) clearance on 1981-06-12, under 510(k) number K810841.

Who is the listed applicant for MEDAID?

The FDA 510(k) record lists C.V.I., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDAID?

The FDA product code for MEDAID is GZJ.

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Other records listing C.V.I., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K811686SURGICAL INSTRUMENTS

Related Devices (Code: GZJ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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